Beijing Key Laboratory of Pediatric Hematology Oncology; National Key Discipline of Pediatrics (Capital Medical University); Key Laboratory of Major Diseases in Children, Ministry of Education; Hematology Oncology Center; Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Hematology and Oncology Laboratory, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Am J Hematol. 2018 Jul;93(7):913-920. doi: 10.1002/ajh.25124. Epub 2018 May 15.
Acute lymphoblastic leukemia (ALL) is the most common malignancy among children. The trial Chinese Children Leukemia Group (CCLG)-ALL 2008 was a prospective clinical trial designed to improve treatment outcome of childhood ALL through the first nation-wide collaborative study in China. Totally 2231 patients were recruited from ten tertiary hospitals in eight cities. The patients were stratified according to clinical-biological characteristics and early treatment response. Standard risk (SR) and intermediate risk (IR) groups were treated with a modified BFM based protocol, and there was 25%-50% dose reduction during intensification phases in the SR group. Patients in high risk (HR) group received a more intensive maintenance treatment. Minimal residual disease (MRD) monitoring with treatment adjustment was performed in two hospitals (the MRD group). Complete remission (CR) was achieved in 2100 patients (94.1%). At five years, the estimate for overall survival (OS) and event-free survival (EFS) of the whole group was 85.3% and 79.9%, respectively. The cumulative incidence of relapse (CIR) was 15.3% at five years. The OS, EFS and CIR for the SR group were 91.5%, 87.9%, and 9.7%, respectively. The outcome of the MRD group is better than the non-MRD group (5y-EFS: 82.4% vs 78.3%, P = .038; 5y-CIR: 10.7% vs 18.0%, P < .001). Our results demonstrated that the large-scale multicenter trial for pediatric ALL was feasible in China. Dose reduction in the SR group could achieve high EFS. MRD-based risk stratification might improve the treatment outcome for childhood ALL.
急性淋巴细胞白血病(ALL)是儿童中最常见的恶性肿瘤。中国儿童白血病协作组(CCLG)ALL2008 是一项前瞻性临床试验,旨在通过中国首次全国性协作研究来提高儿童 ALL 的治疗效果。该试验共纳入了来自中国 8 个城市的 10 家三甲医院的 2231 名患者。这些患者根据临床生物学特征和早期治疗反应进行分层。标准风险(SR)和中危风险(IR)组采用改良 BFM 方案治疗,在强化阶段 SR 组的剂量减少 25%-50%。高危(HR)组患者接受更强化的维持治疗。两所医院(MRD 组)进行了微小残留病(MRD)监测和治疗调整。2100 例患者达到完全缓解(CR)(94.1%)。五年时,全组患者的总生存(OS)和无事件生存(EFS)估计值分别为 85.3%和 79.9%。五年时累积复发率(CIR)为 15.3%。SR 组的 OS、EFS 和 CIR 分别为 91.5%、87.9%和 9.7%。MRD 组的预后优于非-MRD 组(5 年 EFS:82.4%比 78.3%,P=0.038;5 年 CIR:10.7%比 18.0%,P<0.001)。结果表明,在中国开展儿童 ALL 的大规模多中心试验是可行的。SR 组的剂量减少可以实现高 EFS。基于 MRD 的危险分层可能改善儿童 ALL 的治疗效果。